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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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retinitis pigmentosa, juvenile, aipl1-related
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C565778 |
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obsolete hypertrichosis lanuginosa congenita
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7786.0 |
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gelsolin type lattice corneal dystrophy
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C000657784 |
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type II lattice corneal dystrophy
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C000657784 |
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corneal dystrophy, lattice type II
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C000657784 |
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capillary hemangioma, lobular
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D017789 |
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type 2b loeys-dietz syndrome
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C537783 |
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plasmodium falciparum malaria
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D016778 |
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susceptibility to malignant hyperthermia 1
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7783 |
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aphalangia syndactyly microcephaly
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C537787 |
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Intermediate hereditary motor and sensory neuropathy
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18778 |
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macrocephaly with multiple epiphyseal dysplasia and distinctive facies
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11778 |
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papular epidermal nevi with skyline basal cell layers syndrome
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17785 |
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Hodgkin lymphoma nodular LP, NOS
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44778 |
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Hodgkin lymphoma nodular lymphocyte predominant type, NOS
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44778 |
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